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Derma Stretch

EUDAMED

Class I (EU MDR)

Ref 42515MModel GUANTO IN VINILE

by Bericah S.p.A.

Identity

Trade Name
DERMA STRETCH EUDAMED
Device Name
GUANTO MONOUSO IN VINILE SENZA POLVERE NON STERILE EUDAMED
Model / Reference
GUANTO IN VINILE EUDAMED
42515M EUDAMED

Identifiers

Primary DI / UDI-DI
08024151806450 EUDAMED
Basic UDI-DI
8024151GUVSZQ EUDAMED
Direct Marketing DI
08024151806450 EUDAMED
EMDN Code
T01020201 VINYL EXAMINATION / TREATMENT GLOVES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Derma Stretch by Bericah S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bericah S.p.A.
EUDAMED SRN
IT-MF-000007397

Sources (1)

  • EUDAMED 70fd1731-2b20-46d9-ab38-802275529fa7 61 fields · synced Jun 18, 2026